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FDA 510(k)

MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH

K-Number: K760785 · 1976-11-01

Decision Date1976-11-01
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH is the device name listed in this FDA 510(k) record. The listed applicant is Heyer Schulte Corp.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760785. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH?

MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Heyer Schulte Corp.. The 510(k) number is K760785.

When did MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH receive FDA 510(k) clearance?

MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760785.

Who is the listed applicant for MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH?

The FDA 510(k) record lists Heyer Schulte Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH?

The FDA product code for MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH is JXG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Heyer Schulte Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 9 devices →

Related Devices (Code: JXG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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